Clinical Trials Directory

Trials / Unknown

UnknownNCT01404637

Effects of Tamsulosin 0.4mg on Clinical Outcomes in Korean Men With Severe Symptomatic Benign Prostatic Hyperplasia (BPH)

The Effects of Tamsulosin 0.4mg on Clinical Outcomes in Korean Men With Severe Symptomatic BPH

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Samsung Medical Center · Academic / Other
Sex
Male
Age
45 Years – 80 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare the efficacy and safety of tamsulosin 0.4mg (Harnal® D. 0.2mg, 2T) with tamsulosin 0.2mg (Harnal® D 0.2mg, 1T) in patients with severe symptomatic benign prostatic hyperplasia as a first line therapy.

Conditions

Interventions

TypeNameDescription
DRUGTamsulosin 0.4mgTreatment: tamsulosin 0.2mg (2T) /day Posology: two 0.2 mg tablet to be taken after an evening meal.
DRUGTamsulosin 0.2mgtamsulosin 0.2mg (1T) /day Posology: one tablet to be taken after an evening meal.

Timeline

Start date
2011-07-01
Primary completion
2013-07-01
Completion
2013-10-01
First posted
2011-07-28
Last updated
2011-08-02

Source: ClinicalTrials.gov record NCT01404637. Inclusion in this directory is not an endorsement.